Drug profile

The FDA adverse-event record for Divested Suanovil 50

111 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Divested Suanovil 50. See the species affected, top reactions, and outcomes below.

111
adverse-event reports
16.2%
death-coded share
Dog
most-reported species
29
Vomiting - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
111
Total Reports
18
Deaths Reported
16.2%
Death Rate

Active Ingredients

Divested Suanovil 50

Administration Routes

UnknownOralIntramuscularAuricular (Otic)Immersion

Species Affected

Dog 89
Cattle 11
Horse 6
Cat 5

Most Affected Breeds

Retriever - Labrador 12
Terrier - Yorkshire 7
Cattle (other) 6
Terrier - Boston 6
Pit Bull 6
Quarter Horse 6
Shepherd Dog - German 6
Retriever - Golden 5
Chihuahua 5
Domestic Shorthair 5

Most Reported Reactions

Vomiting 29
Lethargy (see also Central nervous system depression in 'Neurological') 14
Seizure NOS 13
Death 11
Hyperglycaemia 10
Anorexia 9
Diarrhoea 8
Dehydration 8
Death by euthanasia 7
Elevated serum alkaline phosphatase (SAP) 7
Lack of efficacy - NOS 6
Lack of efficacy (endoparasite) - heartworm 6

Outcome Breakdown

Outcome Unknown
53 (44.9%)
Recovered/Normal
35 (29.7%)
Died
12 (10.2%)
Ongoing
9 (7.6%)
Euthanized
6 (5.1%)
Recovered with Sequela
3 (2.5%)

Divested Suanovil 50 Adverse Event Insights

111 reports name Divested Suanovil 50; 18 recorded a death outcome (16.2% of reported events, not a population-level mortality rate). Active ingredient: Divested Suanovil 50. Administration routes: Unknown, Oral, Intramuscular, Auricular (Otic).

By species: Dog (89 reports), Cattle (11 reports), Horse (6 reports). By breed: Retriever - Labrador (12), Terrier - Yorkshire (7), Cattle (other) (6).

Leading clinical signs: Vomiting (29), Lethargy (see also Central nervous system depression in 'Neurological') (14), Seizure NOS (13), Death (11). Outcome, 118 coded reports: Outcome Unknown leads at 44.9%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.